Status:

COMPLETED

Mechanisms of Increased Ambulatory Blood Pressure in Patients With Intradialytic Hypertension

Lead Sponsor:

University of Texas Southwestern Medical Center

Collaborating Sponsors:

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Conditions:

Intradialytic Hypertension

Eligibility:

All Genders

18-80 years

Brief Summary

The purpose of this study is 1) to determine what physiologic factors (extracellular fluid overload or vasoconstriction) contribute more to increased blood pressure levels between dialysis treatments ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria (for Aims 1 and 2):
  • age more than 18 years
  • Hypertension defined as systolic blood pressure more than 140 mmHg before dialysis or more than 130 mmHg after dialysis
  • For case subjects with intradialytic hypertension: systolic blood pressure increase more than 10 mmHg from pre to post dialysis in at least 4 out of 6 screening treatments
  • For control subjects: systolic blood pressure decrease more than 10 mmHg from pre to post dialysis in at least 4 out of 6 screening treatments
  • Inclusion criteria for Aim 3 includes the case subjects described above.
  • Exclusion Criteria:
  • For Aims 1 and 2:
  • Hemodialysis vintage less than 1 month
  • Amputated arm or leg
  • Presence of cardiac defibrillator or pacemaker
  • Presence of large metal prosthesis
  • Failure to achieve dry weight
  • For Case subjects participating in Aim 3:
  • Patients with a specific indication for beta blocker therapy including systolic heart failure, history of myocardial infarction, history of tachyarrhythmia or angina being managed with beta blocker therapy.
  • Patients with contraindications to beta blockade including bradycardia (heart rate less than 60 beats per minute) while not on a pulse lowering drug, severe reactive airway disease, prior intolerance to beta blocker therapy
  • Prior intolerance to alpha blocker therapy

Exclusion

    Key Trial Info

    Start Date :

    January 1 2013

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    April 1 2018

    Estimated Enrollment :

    76 Patients enrolled

    Trial Details

    Trial ID

    NCT01862497

    Start Date

    January 1 2013

    End Date

    April 1 2018

    Last Update

    May 1 2018

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University of Texas Southwestern Medical Center at Dallas

    Dallas, Texas, United States, 75390